Thermo Fisher Scientific MEGF10 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA5144703 | - | Thermo Fisher Scientific PA5144703 MEGF10 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 911,000원 | - | 1,002,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence. Antigen range: 285-431. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MEGF10,
uniProtId:
Q96KG7-1,
ncbiNodeId:
9606,
antigenRange:
285-431,
antigenLength:
1140,
antigenImageFileName:
PA5-144703_MEGF10_Q96KG7-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-144703_MEGF10_Q96KG7-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.05 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_3092136
Product Specific Information
Immunogen sequence: NGGTCDAATG QCHCSPGYTG ERCQDECPVG TYGVLCAETC QCVNGGKCYH VSGACLCEAG FAGERCEARL CPEGLYGIKC DKRCPCHLEN THSCHPMSGE CACKPGWSGL YCNETCSPGF YGEACQQICS CQNGADCDSV TGKCTCA
Antigen sequence identity: Mouse 93%; Rat 93%
Target Information
This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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